
doi: 10.1159/000072838
pmid: 14526164
The purpose of this review is to discuss the potential role of “transcriptional therapy” to modulate the expression of target genes in order to treat monogenic as well as multifactorial disorders. In vitro and in vivo experiments with DNA demethylating and histone hyperacetylating drugs are currently performed in several laboratories on a variety of genes. In attempting to place these results into perspective, we divided the target genes into four major categories: (1) single genes with a hypermethylated CpG island; (2) single genes without a CpG island; (3) groups of genes silenced by aberrant DNA methylation; and (4) groups of genes silenced by lack of histone acetylation. We discuss the latest advances in the field of chromatin regulation and, in particular, the role of histone methylation and that of RNA interference in gene silencing. We can expect that in the future regulation of transcription will become an effective treatment for several genetic conditions.
Transcriptional Activation, Acetylation, DNA Methylation, Methylation, Chromatin, Histone Deacetylases, Histone Deacetylase Inhibitors, Histones, Azacitidine, Humans, CpG Islands, DNA (Cytosine-5-)-Methyltransferases, Gene Silencing, Enzyme Inhibitors
Transcriptional Activation, Acetylation, DNA Methylation, Methylation, Chromatin, Histone Deacetylases, Histone Deacetylase Inhibitors, Histones, Azacitidine, Humans, CpG Islands, DNA (Cytosine-5-)-Methyltransferases, Gene Silencing, Enzyme Inhibitors
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